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    Properties
    FFDEAD"> General



    Name Epoxyethane
    Chemical formula C2H4O
    Formula weight 44.05 u
    Synonyms Ethylene oxide, dimethylene oxide, oxirane
    SMILES C1CO1
    CAS number 75-21-8
    UN number 1040
    FFDEAD"> Phase behavior
    Melting point 161 K (-112.1 °C)
    Boiling point 283.5 K (10.4 °C)
    Thermal decomposition ? K (? °C)
    Triple point 160.6 K (-112.4 °C)

    ? kPa
    Critical point 468.9 K (195.9 °C)

    72.3 kPa
    Δfus''H'' 5.17 kJ/mol
    Δfus''S'' 32.2 J/(mol·K)
    Δvap''H'' 25.5 kJ/mol
    Solubility Miscible with water.
    FFDEAD"> Liquid properties
    Δf''H''0liquid -96 kJ/mol
    ''S''0liquid 149.45 J/mol·K)
    ''C''p 86.9 J/(mol·K)
    Density 0.899 ×103 kg/m3
    FFDEAD"> Gas properties
    Δf''H''0gas -52.6 kJ/mol
    ''S''0gas 243 J/(mol·K)
    ''C''p 47 J/(mol·K)
    FFDEAD"> Safety
    Acute effects Lung irritation, convulsions.
    Chronic effects CNS damage
    Potential carcinogen
    Flash point -55 °C
    Autoignition temperature 429 °C
    Explosive limits 3 to 100%
    FFDEAD"> More info
    Properties NIST WebBook
    MSDS Hazardous Chemical Database
    FFDEAD">
    SI units were used where possible. Unless otherwise stated, standard conditions were used.

    Disclaimer and references



    The chemical compound ethylene oxide is an important industrial chemical used as an intermediate in the production of ethylene glycol and other chemicals, and as a sterilant for foodstuffs and medical supplies. It is a colorless flammable gas or refrigerated liquid with a faintly sweet odor. It is the simplest example of an epoxide.

    Its IUPAC name is epoxyethane. Other names for it include oxirane and dimethylene oxide.


        Ethylene oxide
            History
            Production
            Uses
                Reactions
            Health effects
            See also

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    History

    Ethylene oxide was first prepared in 1859 by the French chemist Charles-Adolphe Wurtz, who prepared it by treating 2-chloroethanol with a base. It achieved industrial importance during World War I as a precursor to both the coolant ethylene glycol and the chemical weapon mustard gas. In 1931, Theodore Lefort, another French chemist, discovered a means to prepare ethylene oxide directly from ethylene and oxygen, using silver as a catalyst. Since 1940, almost all ethylene oxide produced industrially has been made using this method.

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    Production

    Industrially, ethylene oxide is produced when ethylene and oxygen react on a silver catalyst at 200–300 °C. Pressures used are in the region of 1-2MPa. The chemical equation for this reaction is

    CH2=CH2 + ½ O2 → C2H4O


    The typical yield for this reaction is 70-80%, the major side reaction being combustion of ethylene to produce carbon dioxide. Several methods to produce ethylene oxide more selectively have been proposed, but none have achieved industrial importance.

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    Uses

    Ethylene oxide gas kills bacteria (and their endospores), mold, and fungi, and can therefore be used to sterilize substances that would be damaged by sterilizing techniques such as pasteurization that rely on heat. Ethylene oxide sterilization for the preservation of spices was patented in 1938 by the American chemist Lloyd Hall, and it is still used in that role. Additionally, ethylene oxide is widely used to sterilize medical supplies such as bandages, sutures, and surgical implements.

    Most ethylene oxide, however, is used as an intermediate in the production of other chemicals. The major use of ethylene oxide is in the production of ethylene glycol, which is widely used as an automotive coolant and antifreeze, and is also used to produce polyester polymers.

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    Reactions

    Most reactions are ring openings by nucleophiles.

    In industry, epoxyethane is reacted with water in the presence of a sulfuric acid catalyst. A ten-fold molar excess of water is used to obtain ethylene glycol:

    C2H4O + H2O → HOCH2CH2OH

    Despite the large excess of water, various types of polyethylene glycol (PEG) or polyethylene oxide (PEO) are still formed as secondary products. The degree of polymerization increases as a smaller proportion of water is used:

    n(CH2CH2O) + H2O → HO(CH2CH2O)nH

    For example, under the right conditions it can give diethylene glycol (HOCH2CH2OCH2CH2OH), triethylene glycol, etc.

    Similarly, reaction with ammonia can yield ethanolamine, diethanolamine, or triethanolamine.

    Ethylene oxide is also important in the manufacture of surfactants and other detergents, in a process called ethoxylation.

    One class of ethylene oxide derivatives that has attracted much scientific attention is the crown ethers, which are cyclic oligomers of ethylene oxide. These compounds have the ability to make ionic compounds such as salts soluble in nonpolar solvents which they otherwise could not dissolve in. However, the high cost of these compounds has largely confined their use to the laboratory rather than industrial practice.

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    Health effects

    Ethylene oxide is toxic by inhalation. Symptoms of overexposure include headache and dizziness, progressing with increasing exposure to convulsions, seizure and coma. It is also an irritant to skin and the respiratory tract, and inhaling the vapors may cause the lungs to fill with fluid several hours after exposure.

    Ethylene oxide is usually stored as a pressurized or refrigerated liquid. At room temperature and pressure, it rapidly evaporates, potentially causing frostbite in cases of skin exposure.

    Laboratory animals exposed to ethylene oxide for their entire lives have had a higher incidence of liver cancer. However, studies on human beings who have worked with ethylene oxide for extended periods and may have experienced low doses during that time have found no increase in cancer risk. Chronic ethylene oxide exposure may increase the risk of cataracts in humans.

    In animals, ethylene oxide can cause numerous reproductive effects, including mutations and a higher rate of miscarriages. Its reproductive effects on humans have not been well studied, but it is considered probable that ethylene oxide exposure has similar effects on human reproduction.

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    See also

     
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    This article is licensed under the GNU Free Documentation License [copyleft]. It uses material from the Wikipedia article "Ethylene oxide". link